NDC 0642-0070

Vitafol One

Prenatal Supplement With Dha

Vitafol One is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Everett Laboratories, Inc.. The primary component is Vitamin A; Ascorbic Acid; Thiamine Mononitrate; Riboflavin; Niacin; Pyridoxine Hydrochloride; Cyanocobalamin; Folic Acid; Iodine; Magnesium; Zinc; Copper; Vitamin D; Omega-3 Fatty Acids; .alpha.-tocopherol; Iron.

Product ID0642-0070_50262876-4ef2-4eda-9b5e-f586a8bb7ce4
NDC0642-0070
Product TypeHuman Prescription Drug
Proprietary NameVitafol One
Generic NamePrenatal Supplement With Dha
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date2011-06-13
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameEverett Laboratories, Inc.
Substance NameVITAMIN A; ASCORBIC ACID; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; FOLIC ACID; IODINE; MAGNESIUM; ZINC; COPPER; VITAMIN D; OMEGA-3 FATTY ACIDS; .ALPHA.-TOCOPHEROL; IRON
Active Ingredient Strength330 ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1
Pharm ClassesVitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Vitamin D [CS],Vitamin D [EPC],Fatty Acids, Omega-3 [CS],Omega-3 Fatty Acid [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0642-0070-01

1 BLISTER PACK in 1 BOX (0642-0070-01) > 4 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Marketing Start Date2011-06-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0642-0070-30 [00642007030]

Vitafol One CAPSULE, GELATIN COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-06-13
Inactivation Date2020-01-31

NDC 0642-0070-01 [00642007001]

Vitafol One CAPSULE, GELATIN COATED
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-06-13
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
VITAMIN A1100 [iU]/1

OpenFDA Data

SPL SET ID:42a5cafd-a2c0-4ac2-99c9-708642f00716
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1119573
  • 1119569
  • Pharmacological Class

    • Vitamin C [EPC]
    • Ascorbic Acid [CS]
    • Vitamin B6 Analog [EPC]
    • Vitamin B 6 [Chemical/Ingredient]
    • Analogs/Derivatives [Chemical/Ingredient]
    • Vitamin B 12 [CS]
    • Vitamin B12 [EPC]
    • Vitamin D [CS]
    • Vitamin D [EPC]

    Trademark Results [Vitafol]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    VITAFOL
    VITAFOL
    88294273 not registered Live/Pending
    EXELTIS USA INC.
    2019-02-08
    VITAFOL
    VITAFOL
    86653118 4859841 Live/Registered
    Exeltis USA, Inc.
    2015-06-05
    VITAFOL
    VITAFOL
    73611865 1452861 Live/Registered
    EVERETT LABORATORIES, INC.
    1986-07-28
    VITAFOL
    VITAFOL
    72084824 0728602 Live/Registered
    VITA ZAHNFABRIK H. RAUTER, KG
    1959-11-06

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